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    Understanding and Implementing a Quality by Design Program

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    Website https://worldcomplianceseminars.com/upcoming_webinar | Want to Edit it Edit Freely

    Category Sales, Trade compliance, Logistics, Audits, Legal counsel

    Deadline: March 03, 2020 | Date: March 03, 2020

    Venue/Country: U.S.A

    Updated: 2020-01-06 15:01:16 (GMT+9)

    Call For Papers - CFP

    Session Highlights

    • Quality Target Product Profile (QTPP)

    • Risk Assessment

    • Using Models

    • Design of Experiments

    • Developing a Design Space

    • Process Analytical Technology (PAT)

    • FMEA and Control Plan

    • Target Operational Profile

    • Control Strategy

    This training will explain the main principles behind a QbD approach and provide guidelines in how to implement the concepts into a pharmaceutical development organization. Topics covered will include the target product quality profile, risk assessment, methods to establish a design space, and design of a control strategy. This review will help bridge the gap between understanding the principles and practical application.

    Speaker Profile:

    Steven Laurenz– Chemical Engineering M.S. – Michigan State University

    Expertise: Over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.